Zhang Dongmei, Xiao Yi, Luo Jinmei, Wang Xiaona, Qiao Yixian, Huang Rong, Wu Wei
Department of Respiratory Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.
Sleep Breath. 2019 Sep;23(3):785-793. doi: 10.1007/s11325-018-1760-1. Epub 2018 Dec 12.
Airway inflammation plays an important role in obstructive sleep apnea (OSA); exhaled nitric oxide is regarded as a noninvasive marker of airway inflammation. The aim of this study was to evaluate fractional exhaled nitric oxide (FeNO) and nasal nitric oxide (nNO) in patients with OSA.
Seventy-five patients with OSA and 30 health controls were enrolled in this study. FeNO and nNO were measured before and after sleep. Nasal lavage was performed in 31 non-smoking individuals immediately after NO measurement in the morning. The sample of nasal lavage was taken for cell classification and analyzing interleukin 6 (IL-6) and interleukin 8 (IL-8).
Both FeNO and nNO were significantly higher in OSA (before sleep FeNO 21.08 ± 8.79 ppb vs.16.90 ± 6.86 ppb, p = 0.022; after sleep FeNO 25.57 ± 15.58 ppb vs.18.07 ± 6.25 ppb, p = 0.003; before sleep nNO 487.03 ± 115.83 ppb vs. 413.37 ± 73.10 ppb, p = 0.001; after sleep nNO 550.07 ± 130.24 ppb vs. 460.43 ± 109.77 ppb, p < 0.001). Furthermore, in non-smoking OSA, nNO levels were positively correlated with apnea hypopnea index (AHI) and average decrease of pulse arterial oxygen saturation (SpO); after sleep, nNO was also positively associated to recording time with SpO < 90% and negatively associated to minimum SpO. Both before and after sleep nNO levels were positively correlated with the percentage of neutrophils in nasal lavage (r = 0.528, p = 0.014; r = 0.702, p < 0.001, respectively). Additionally, before sleep nNO was also positively associated with IL-6 (r = 0.586, p = 0.005) and IL-8 (r = 0.520, p = 0.016) concentration.
This study sustains the presence of airway inflammation in OSA patients with the increase of FeNO and nNO. The data suggests nNO might have greater value than FeNO since it positively correlated with OSA severity, and nNO is a potential bio-marker of nasal inflammation in non-smoking OSA patients.
气道炎症在阻塞性睡眠呼吸暂停(OSA)中起重要作用;呼出一氧化氮被视为气道炎症的无创标志物。本研究旨在评估OSA患者的呼出气一氧化氮分数(FeNO)和鼻一氧化氮(nNO)。
本研究纳入了75例OSA患者和30名健康对照者。在睡眠前后测量FeNO和nNO。31名非吸烟个体在早晨测量NO后立即进行鼻腔灌洗。采集鼻腔灌洗样本进行细胞分类,并分析白细胞介素6(IL-6)和白细胞介素8(IL-8)。
OSA患者的FeNO和nNO均显著升高(睡眠前FeNO 21.08±8.79 ppb vs.16.90±6.86 ppb,p = 0.022;睡眠后FeNO 25.57±15.58 ppb vs.18.07±6.25 ppb,p = 0.003;睡眠前nNO 487.03±115.83 ppb vs. 413.37±73.10 ppb,p = 0.001;睡眠后nNO 550.07±130.24 ppb vs. 460.43±109.77 ppb,p < 0.001)。此外,在非吸烟的OSA患者中,nNO水平与呼吸暂停低通气指数(AHI)和脉搏动脉血氧饱和度(SpO)的平均下降呈正相关;睡眠后,nNO也与SpO < 90%的记录时间呈正相关,与最低SpO呈负相关。睡眠前后nNO水平均与鼻腔灌洗中性粒细胞百分比呈正相关(r = 0.528,p = 0.014;r = 0.702,p < 0.001)。此外,睡眠前nNO还与IL-6(r = 0.586,p = 0.005)和IL-8(r = 0.520,p = 0.016)浓度呈正相关。
本研究通过FeNO和nNO的升高证实了OSA患者存在气道炎症。数据表明nNO可能比FeNO具有更大的价值,因为它与OSA严重程度呈正相关,并且nNO是非吸烟OSA患者鼻腔炎症的潜在生物标志物。